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Cancer of the Adrenal Gland in Children: Experience at the M.D. Anderson Hospital and Tumor Institute

  • Norman Jaffe
  • Ayten Cangir
Part of the Cancer Treatment and Research book series (CTAR, volume 17)

Abstract

Adrenal cortical carcinoma is a rare neoplasm in infancy. Most cases present with Cushing’s syndrome, hirsuitism, precocious puberty, or rarely inappropriate ADH secretion. Associated congenital anomalies and concurrent central nervous system and hepatic tumors have also been documented. Occasionally, the tumor may be non-functioning. Three cases have been seen at the M.D. Anderson Hospital and Tumor Institute with a variety of presentations and outcome.

Keywords

Precocious Puberty Adrenal Cortical Carcinoma Tumor Institute Primiparous Mother Anderson Hospital 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. 1.
    Visconti EB, Peters RW, Cangir A, Zorn GL Jr, Fisher S: Unusual case of Adrenal Cortical Carcinoma in a female infant. Arch Dis Child 53: 342–344, 1978.PubMedCrossRefGoogle Scholar

Copyright information

© Martinus Nijhoff Publishers, Boston 1983

Authors and Affiliations

  • Norman Jaffe
  • Ayten Cangir

There are no affiliations available

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